Takotsubo-like cardiomyopathy in a 17-year-old male with a pheochromocytoma.

Pediatr Cardiol

Pediatric Cardiology Department, The University of Iowa Children's Hospital, 200 Hawkins Drive, Iowa City, IA 52240, USA.

Published: February 2009

We report a case of a 17-year-old adolescent male with Takotsubo-like cardiomyopathy in the setting of pheochromocytoma who presented with hematemesis, hypertension, and pallor. Takotsubo-like cardiomyopathy is rarely reported in the pediatric population, and this is the first report in the pediatric literature of Takotsubo-like cardiomyopathy associated with both pheochromocytoma and an elongated course of the left anterior descending coronary artery.

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http://dx.doi.org/10.1007/s00246-008-9279-zDOI Listing

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Article Synopsis
  • Pheochromocytoma is a rare tumor that secretes catecholamines and can cause severe symptoms like high blood pressure, rapid heart rate, headaches, and sweating; timely diagnosis is crucial to prevent complications.
  • A case study of a 25-year-old woman showed she presented with hypertensive encephalopathy and acute coronary syndrome linked to pheochromocytoma, which was later confirmed via imaging and biochemical tests.
  • After targeted treatment and surgery to remove the tumor, the patient’s hypertension and symptoms fully resolved, underscoring the need to consider pheochromocytoma in cases of acute neurological and cardiac issues.
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